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rs397516170

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516170(A;A)
Make rs397516170(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424050
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516170
ebirs397516170
HLIrs397516170
Exacrs397516170
Varsomers397516170
Maprs397516170
PheGenIrs397516170
hapmaprs397516170
1000 genomesrs397516170
hgdprs397516170
ensemblrs397516170
gopubmedrs397516170
geneviewrs397516170
scholarrs397516170
googlers397516170
pharmgkbrs397516170
gwascentralrs397516170
openSNPrs397516170
23andMers397516170
23andMe allrs397516170
SNP Nexus

SNPshotrs397516170
SNPdbers397516170
MSV3drs397516170
GWAS Ctlgrs397516170
Max Magnitude0
ClinVar
Risk rs397516170(A;A)
Alt rs397516170(A;A)
Reference rs397516170(G;G)
Significance Probable-Pathogenic
Disease not specified Familial hypertrophic cardiomyopathy 1
Variation info
Gene MYH7
CLNDBN not specified Familial hypertrophic cardiomyopathy 1
Reversed 1
HGVS NC_000014.8:g.23893259C>T
CLNSRC
CLNACC RCV000035825.2, RCV000168878.1,